Aastrom Biosciences, Inc.
Table of Contents

 
 
UNITED STATES SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
 
Form 8-K
CURRENT REPORT
PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
Date of report (date of earliest event reported):
February 7, 2007
Aastrom Biosciences, Inc.
(Exact name of registrant as specified in its charter)
         
Michigan
(State or other jurisdiction of
incorporation)
  0-22025
(Commission File No.)
  94-3096597
(I.R.S. Employer
Identification No.)
24 Frank Lloyd Wright Drive
P.O. Box 376
Ann Arbor, Michigan 48106

(Address of principal executive offices)
Registrant’s telephone number, including area code:
(734) 930-5555
 
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
o Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
o Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
o Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
o Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
 
 

 


TABLE OF CONTENTS

Item 2.02 Results of Operations and Financial Condition.
Item 9.01 Financial Statements and Exhibits.
SIGNATURES
EXHIBIT 99.1


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Item 2.02 Results of Operations and Financial Condition.
On February 7, 2007, we issued a press release announcing financial results and achievements for our second fiscal quarter ended December 31, 2006. A copy of the press release is attached hereto as Exhibit 99.1.
Pursuant to General Instruction B.2 of Form 8-K, this report and the exhibit are not deemed to be “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, nor shall this report and the exhibit be incorporated by reference into our filings under the Securities Act of 1933 or the Securities Exchange Act of 1934, except as expressly set forth by specific reference in such future filing.
Item 9.01 Financial Statements and Exhibits.
     (d) Exhibits.
     
Exhibit No.   Description
99.1
  Press Release dated February 7, 2007

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SIGNATURES
     Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
Date: February 7, 2007
         
  AASTROM BIOSCIENCES, INC.
 
 
  By:   /s/ Gerald D. Brennan, Jr.    
    Gerald D. Brennan, Jr.   
    Vice President Administrative & Financial Operations and CFO   
 

3

Exhibit 99.1
 

EXHIBIT 99.1
(Aastrom Logo)
FOR IMMEDIATE RELEASE
         
CONTACTS:
  Kris M. Maly
Investor Relations Department
Aastrom Biosciences, Inc.
Phone: (734) 930-5777
  Cameron Associates
Kevin McGrath
Phone: (212) 245-4577
Deanne Eagle (Media)
Phone: (212) 554-5463
Aastrom Reports Second Quarter Fiscal Year 2007 Financial Results
Ann Arbor, Michigan, February 7, 2007 — Aastrom Biosciences, Inc. (Nasdaq: ASTM), a company developing cell-based therapeutics for regenerative medicine, today reported financial results for the second fiscal quarter ended December 31, 2006. The Company also reported operational achievements during the quarter, including:
    Senior management appointments
    Ronnda L. Bartel, Ph.D. as Vice President, Research & Development. Dr. Bartel is responsible for the product development and manufacturing of Aastrom’s Tissue Repair Cell-based (TRC) cell products, and the Company’s discovery and research efforts.
 
    Sheldon A Schaffer, Ph.D. as Vice President, Corporate Development & Intellectual Property, a newly created position. Dr. Schaffer is responsible for the development of corporate partnering and licensing opportunities, as well as the expansion of Aastrom’s intellectual property portfolio.
In addition, the Company has achieved the following clinical milestones during fiscal year 2007:
    Completed patient enrollment in the EU Phase I/II long bone fracture clinical trial
 
    Initiated patient enrollment and treatments in the pivotal osteonecrosis clinical trial in Spain
 
    Received Orphan Drug Designation from the FDA for the treatment of dilated cardiomyopathy
“During this fiscal year we have strengthened our management team and accomplished several key clinical milestones. Each of these milestones are critical to achieving our overall corporate goal of advancing our clinical programs through the regulatory process and delivering cell therapies for regenerative medicine,” said George Dunbar, Chief Executive Officer and Chairman of Aastrom. “Since the beginning of calendar year 2007, we have initiated and treated patients in our adult stem cell clinical trial for osteonecrosis in Spain, and received an orphan drug designation from the FDA for dilated cardiomyopathy, a severe chronic disease of the heart. We look forward to reporting on the clinical progress we have planned for the remainder of 2007.”
Second Fiscal Quarter Ended December 31, 2006 Results
Total revenues for the quarter and six months ended December 31, 2006, consisting of limited therapy kit sales for research by others and grant funding, were $158,000 and $262,000, respectively, compared to $117,000 and $297,000 for the same periods in fiscal year 2006.
Total costs and expenses for the quarter and six months ended December 31, 2006 increased to $4,898,000 and $9,586,000, respectively, from $4,456,000 and $8,430,000 for the same periods in fiscal year 2006.
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(Aastrom Letterhead)

 


 

Aastrom- 2nd Q FY2007 Fin Results
February 7, 2007
Page 2
Research and development expenses for the quarter and six months ended December 31, 2006 increased to $2,563,000 and $4,867,000, respectively, from $2,195,000 and $4,148,000 for the same periods in fiscal year 2006. These increases reflect continued expansion of our research and development activities to support future regulatory submissions, on-going and planned tissue regeneration clinical trials in the U.S. and EU and the development of facilities for product manufacturing. Research and development expenses for the quarter and six months ended December 31, 2006, also include a non-cash charge of $181,000 and $290,000, respectively, compared to $121,000 and $199,000 for the same periods in fiscal year 2006, relating to share-based compensation expense.
Selling, general and administrative costs for the quarter and six months ended December 31, 2006 increased to $2,332,000 and $4,716,000, respectively, from $2,257,000 and $4,273,000 for the same periods in fiscal year 2006. For the quarter and six months ended December 31, 2006, these increases include a non-cash charge of $690,000 and $1,152,000, respectively, compared to $185,000 and $303,000 for the same periods in fiscal year 2006, relating to share-based compensation expense. The increases in non-cash charges include a one-time non-cash charge of $257,000 that relates to an amendment of the former CEO’s consulting agreement. In addition, for the six months ended December 31, 2006, the increase includes an accrual relating to the former CEO’s revised employment agreement, and an accrual and severance payments relating to the former President and COO’s employment agreement.
Interest income for the quarter and six months ended December 31, 2006 increased to $515,000 and $1,042,000, respectively, from $197,000 and $503,000 for the same periods in fiscal year 2006. The fluctuations in interest income are due primarily to corresponding changes in the level of cash, cash equivalents and short-term investments during the periods, and to improved yields from our investments.
Net loss for the quarter ended December 31, 2006 was $4,225,000, or $.04 per share, compared to a net loss of $4,142,000, or $.04 per share for the same period in fiscal year 2006. Net loss for the six months ended December 31, 2006, was $8,282,000, or $.07 per share, compared to $7,630,000, or $.07 per share for the same period in fiscal year 2006. The increases in net loss are primarily the result of increased costs and expenses offset on a per share basis by an increase in the weighted average number of common shares outstanding.
At December 31, 2006, the Company had $36.3 million in cash, cash equivalents and short-term investments as compared to $43 million at June 30, 2006.
Aastrom Conference Call Information
George W. Dunbar, President and Chief Executive Officer, Gerald D. Brennan, Jr., Vice President Administrative & Financial Operations and Chief Financial Officer, and Elmar R. Burchardt, M.D., Ph.D., Vice President Medical Affairs of Aastrom Biosciences, Inc., will host a conference call to review and discuss the second quarter fiscal year 2007 financial results at 9:00 a.m. (EST) today, February 7, 2007. Interested parties should call toll-free (877) 407-9205, or from outside the U.S. (201) 689-8054, fifteen minutes before the start of the call to register and identify themselves as registrants of the ‘Aastrom Conference Call’. Any registered caller on the toll-free line may ask to be placed in the queue for the Question & Answer session. The call will be simulcast on the web at http://www.vcall.com/IC/CEPage.asp?ID=113519. A podcast of the call may be downloaded from the web at the internet address above. If you are unable to participate during the live call, the webcast will be available for replay at http://www.investorcalendar.com/ for 60 days. Also, through February 17, 2007, an audio replay of the call will be available by dialing toll-free (877) 660-6853, or from outside the U.S. (201) 612-7415; when prompted on the phone line, the Account # is: 286 and the Conference ID# is: 230316.
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Aastrom- 2nd Q FY2007 Fin Results
February 7, 2007
Page 3
About Aastrom Biosciences, Inc.
Aastrom Biosciences, Inc. develops autologous cell products for the repair or regeneration of multiple human tissues, based on its proprietary Tissue Repair Cell (TRC) technology. Aastrom’s TRC-based products are a unique cell mixture containing stem and progenitor cell populations, produced from a small amount of bone marrow taken from the patient. TRC-based products have been used in over 240 patients, and are currently in clinical trials for bone regeneration (osteonecrosis of the femoral head, long bone fractures and spine fusion) and vascular regeneration (critical limb ischemia) applications. Aastrom has reported positive interim clinical trial results for TRCs suggesting both the clinical safety and the ability of TRCs to promote healing in bone regeneration applications. The Company is also developing programs for TRC-based therapies to address cardiac and neural regeneration indications. TRCs have received Orphan Drug Designation from the FDA for use in the treatment of osteonecrosis of the femoral head and the treatment of dilated cardiomyopathy, a severe chronic disease of the heart.
For more information, visit Aastrom’s website at www.aastrom.com. (astmf)
This document contains forward-looking statements, including without limitation, statements concerning clinical trial plans and expectations, intended product development and commercialization objectives, expected milestones, plans for the current fiscal year and potential product applications, which involve certain risks and uncertainties. The forward-looking statements are also identified through use of the words “planned,” “should” and other words of similar meaning. Actual results may differ significantly from the expectations contained in the forward-looking statements. Among the factors that may result in differences are the inherent uncertainties associated with clinical trial and product development activities, regulatory approval requirements, the availability of resources and the allocation of resources among different potential uses. These and other significant factors are discussed in greater detail in Aastrom’s Annual Report on Form 10-K and other filings with the Securities and Exchange Commission.
— Financial Table Follows —

 


 

AASTROM BIOSCIENCES, INC.
(Unaudited)
(In thousands, except per share amounts)
CONSOLIDATED STATEMENTS OF OPERATIONS DATA:
                                 
    Quarter ended December 31,     Six months ended December 31,  
    2005     2006     2005     2006  
REVENUES:
                               
Total revenues
  $ 117     $ 158     $ 297     $ 262  
 
                       
 
                               
COSTS AND EXPENSES:
                               
Cost of product sales
    4       3       9       3  
Research and development
    2,195       2,563       4,148       4,867  
Selling, general and administrative
    2,257       2,332       4,273       4,716  
 
                       
Total costs and expenses
    4,456       4,898       8,430       9,586  
 
                       
 
                               
OTHER INCOME
    197       515       503       1,042  
 
                       
 
                               
NET LOSS
  $ (4,142 )   $ (4,225 )   $ (7,630 )   $ (8,282 )
 
                       
 
                               
NET LOSS PER COMMON SHARE
                               
(Basic and Diluted)
  $ (.04 )   $ (.04 )   $ (.07 )   $ (.07 )
 
                       
 
                               
Weighted average number of common shares outstanding
    102,681       119,516       102,582       119,347  
 
                       
CONSOLIDATED BALANCE SHEET DATA:
                 
    June 30,     December 31,  
    2006     2006  
ASSETS
               
Cash and cash equivalents
  $ 9,034     $ 13,979  
Short-term investments
    33,963       22,333  
Receivables, net
    139       121  
Inventories
    1       12  
Other current assets
    528       518  
Property and equipment, net
    1,216       1,277  
 
           
Total assets
  $ 44,881     $ 38,240  
 
           
 
               
LIABILITIES AND SHAREHOLDERS’ EQUITY
               
Current liabilities
  $ 2,539     $ 2,317  
Shareholders’ equity
    42,342       35,923  
 
           
Total liabilities and shareholders’ equity
  $ 44,881     $ 38,240  
 
           
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